K240185
- 510(k) number
- K240185
- Device name
- Cypris eXact Suture Placement Device
- Applicant
- Cypris Medical IL · US
- Product code
- GEJ — Carrier, Ligature
- Decision date
- 2024-05-03
- Date received
- 2024-01-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K240185.pdf
Official FDA record: K240185
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.